Product Name :HB9/HLXB9/MNX1 Recombinant Rabbit mAb (KU)
Application_all :WB: 1:1000<br />IP: 1:20
Background :This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Product :Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
Purification&Purity :Affinity Purification
Storage&Stability :Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Note :For research use only, not for use in diagnostic procedure.
Alternative Name :HB9; HLXB9; SCRA1; HOXHB9
Immunogen :A synthetic peptide of human HB9/HLXB9/MNX1
Modification :Unmodification
